Warnings
For external use only. If accidentally ingested contact poison control immediately.
Menthol
FDA Label NDC 67285-102
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Relief-mart, Inc for the product Menthol (NDC 67285-102). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.
This specific version of the label includes detailed information regarding warnings, active ingredients, purpose, inactive ingedients, directions, stop use section, uses, pdp, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Active Ingredients
Natural L-Menthol 7.5%
Purpose
Topical Analgesic
Inactive Ingedients
Deionized Water, Isopropyl Alcohol, Oil of Peppermint, Oil of Eucalyptus, Proprietary Skin Conditioner.
Uses
Relieves temporary pain due to
arthiritus
neck and back pains
stiffness
msucle soreness
cramps
sprains and strains
tendonitis
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